insulin shock therapy

insulin shock therapy的基本解释

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胰岛素休克治疗

与insulin shock therapy相关的网络例句 [注：此内容来源于网络，仅供参考]

We then add boundaries delineated forward/backward facing reflected shock, Mechanical equilibrium, M2=1 and reflected shock strong/weak separating conditions on the (M0,q1) map of shih(2004). This is followed by systematically investigating multiply possible three shock theoretical solutions of steady Mach reflections in perfect triatomic gases. Pressure-deflection shock polar solutions are used to help illustrate different solution behaviors of these theoretical three-shock solutions. M0 is flow Mach no. upstream of incident shock, M1 is flow Mach no. downstream of incident shock, M2 is flow Mach no. downstream of reflected shock,q1 is flow deflection downstream of incident shock.

随后本文由石(2004)论文中加入前后分界、机械平衡、M2=1及强弱分界条件，然后有系统地探讨三原子分子理想气体(r=1.2857 )稳态马赫反射参震波理论多重解之交点及其对应之压力-转折角震波极图解，并建构出此三原子分子理想气体稳态马赫反射流场三震波十阶多项式理论解於(Mo，q1)平面上之解域图，其中M0为入射震波上游流场马赫数，M1为入射震波下游流场马赫数，M2为入射震波下游流场马赫数，q1为入射震波下游流场转折角。

RESULTS: Biomaterial vector which were used to coated insulin could prevent insulin degradation by erepsin and enhance insulin stability. In addition, biomaterial vector benefited for uptake and transport of intestinal tract mucosa to insulin, target-control of drug release, enhancement of drug bioavailability, and establishment of insulin release velocity style for human physiological drive so as to realize sustained release of insulin.

结果：以生物材料作为载体包埋胰岛素，可避免胰岛素被胃肠蛋白酶降解，提高其在胃肠道内的稳定性，并有利于肠道黏膜对胰岛素的摄取和转运，在人体内递药过程中又能实现靶向控制药物释放，提高药物的生物利用度，满足人体生理需求的胰岛素的释放速率模式，实现了胰岛素的持续释放。

The results showed as:(1)Gegen decreases fasting insulin and insulin resistance index and increases insulin sensitive index of rats of insulin resistance induced by dexamethasone significantly;(2)Gegen can improve glucose tolerance of rats of insulin resistance but not to alloxan indued diabetes mice;(3)Gegen increases glucose intake of 3T3-L1 adipocytes and improves the insulin resistance of 3T3-L1 adipocytes induced by dexamethasone significantly;(4)Gegen can activate peroxisome proliferator- activated receptor gamma, make it bind to PPAR response elements;(5)Gegen can up-regulate mRNA expression of PPAR v ,aP2 and adiponectin.

结果表明：①葛根显著降低地塞米松诱导的胰岛素抵抗大鼠血清胰岛素水平和胰岛素抵抗指数，升高胰岛素敏感指数，改善大鼠的胰岛素抵抗；②葛根显著改善胰岛素抵抗大鼠的糖耐量，但对四氧嘧啶糖尿病小鼠的糖耐量没有明显的作用；③葛根显著增加胰岛素抵抗3T3-L1脂肪细胞对葡萄糖的摄取，改善地塞米松诱导的3T3-L1脂肪细胞的胰岛素抵抗；④葛根能促进HepG2肝癌细胞过氧化物酶体增殖物激活受体γ与靶基因的特异DNA序列结合，对PPARγ及其下游基因的转录具有激活作用；⑤葛根能够促进PPARγ及其下游基因脂肪酸结合蛋白(aP2)、脂联素mRNA的表达。

与insulin shock therapy相关的网络解释 [注：此内容来源于网络，仅供参考]

insulin shock：胰岛素休克,低血糖休克

insulin release test 胰岛素释放试验 | insulin shock 胰岛素休克,低血糖休克 | insulin shock therapy 胰岛素昏迷疗法,胰岛素休克疗法

insulin shock therapy：胰岛素昏迷疗法,胰岛素休克疗法

insulin shock 胰岛素休克,低血糖休克 | insulin shock therapy 胰岛素昏迷疗法,胰岛素休克疗法 | insulin syringe 胰岛素注射器

insulin shock：胰岛素休克,低血糖休克

insulin release test ==> 胰岛素释放试验 | insulin shock ==> 胰岛素休克,低血糖休克 | insulin shock therapy ==> 胰岛素昏迷疗法,胰岛素休克疗法